Production Operator II

CuriaCamarillo, CA
13h$53,000 - $63,800

About The Position

Production Operator II in Camarillo, CA Build your future at Curia, where our work has the power to save lives  Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives. Summary: Support timely manufacturing of parenteral cGMP products in an aseptic environment including executing and supporting formulation operations in a GMP-regulated environment. This role performs complex processing activities, supports troubleshooting and process improvements, and contributes to documentation development and technical writing efforts to ensure compliant and efficient manufacturing operations.

Requirements

  • Bachelor’s degree in Life Sciences, Engineering, Biotechnology, or related technical field required, or High school diploma or general education degree (GED) and a  minimum of five (5)  years  related industry experience in formulation operations within a GMP-regulated environment.
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
  • Ability to write routine reports and correspondence.
  • Ability to speak effectively before groups of customers or employees of organization.
  • Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
  • Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.
  • Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form.
  • Ability to deal with problems involving several concrete variables in standardized situations.
  • Knowledge of Internet software; Manufacturing software; Spreadsheet software and Word Processing software.
  • Comprehend and follow SOPs, cGMPs, and detailed instructions to successfully produce sterile quality products.
  • Document information, events, and cGMP manufacturing processes clearly, accurately and completely.
  • Perform duties in an organized, detail-oriented manner.
  • Apply basic math: measures, weights, fractions, decimals.
  • Apply basic computer skills.
  • Work and communicate well with others in a team environment.
  • Must pass background check
  • Must pass drug screen
  • Pass Wonderlic Basic Skills Test at 12th grade level or higher

Responsibilities

  • Execute and support complex formulations and compounding operations according to batch records and SOPs.
  • Operate and monitor formulation equipment including mixers, tanks, filtration systems, and transfer systems.
  • Ensure adherence to GMP, safety, and data integrity requirements.
  • Support process scale-up, engineering runs, and GMP batches.
  • Assist in drafting and revising SOPs, batch records, and protocols.
  • Review batch record documentation for accuracy and completeness.
  • Support technical transfer and process documentation updates.
  • Prepare and sanitize equipment for clean rooms, product compounding, and filling according to preparation list, including disassembly/assembly.
  • Load and unload steam sterilizers and washers according to diagrams and instructions.
  • Record all procedures in logbooks following completion and complete/correct batch records.
  • Sanitize aseptic/controlled production areas to ensure microbial contamination is reduced to safe level on inanimate surfaces.
  • Bubble point test filters and read/interpret SOPs to ensure compliance.
  • Other duties as assigned

Benefits

  • Generous benefit options (eligible first day of employment)
  • Paid training, vacation and holidays (vacation accrual begins on first day of employment)
  • Career advancement opportunities
  • Education reimbursement
  • 401K program with matching contributions
  • Learning platform
  • And more!
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